FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
CV Term Report
Help Close All Open All
General Information
Term Parkinson's disease 21 ID (Ontology) DOID:0111251 (Human Disease)
Definition A late onset Parkinson's disease characterized by autosomal dominant inheritance and mean age of onset at 67 years.
Also Known As "PARK21" ; "Parkinson disease 21"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS

Choose a record type to view annotations for this term and its child terms. Direct annotations and full annotation statements below also provide HitList buttons.

  • Results list data from multiple species. Choose a record type above to open its HitList.
Direct annotations: records annotated with this exact term (child terms are NOT included)
Data ClassFieldDirect annotations
Human Disease Models (FBhh)DOID2 (maintenance)
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes Human Disease Models
 Parkinson's disease 21
Spanning Tree (Parents/Children)
Only view relationship:
Vocabulary search: maintenance
autosomal genetic disease
 |__autosomal dominant disease______
Parkinson's disease                 |
 |__late onset Parkinson's disease__|
                                    Parkinson's disease 21  4 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
late onset Parkinson's disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "PARK21" EXACT OMO:0003012
    "Parkinson disease 21" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:616361